restrictive lung disease
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Etiology
- parenchymal disorders
- sarcoidosis
- idiopathic pulmonary fibrosis (50-70 years, most common ILD)
- pneumoconiosis
- hypersensitivity pneumonitis (bird fancier's lung, farmer's lung)
- drug or radiation-induced interstitial lung disease
- amiodarone toxicity
- extra-parenchymal disorders
Laboratory
Diagnostic procedures
- pulmonary function testing
- decreased total lung capacity < 80%
- FEV1/FVC > 75%
- decreased residual volume suggests interstitial lung disease
- increased residual volume suggests neuromuscular disease[2]
Radiology
- chest X-ray may show only low lung volume with neuromuscular disease
- infiltrates suggest interstitial lung disease
- high-resolution computed tomography if pulmonary function testing suggests pathology not revealed by chest X-ray